Literature DB >> 17457517

Fiber specific differential phosphorylation of the alpha1-subunit of the Na(+),K (+)-ATPase in rat skeletal muscle: the effect of aging.

Lianqin Zhang1, Yuk-Chow Ng.   

Abstract

In skeletal muscle, the Na(+),K(+)-ATPase maintains the Na(+) and K(+) gradients and modulates contractile functions. The different fibers of the skeletal muscle possess diverse properties and functions, and thus, the demands for the Na-pump activity might be different. Because phosphorylation of the alpha1-subunit of the Na(+),K(+)-ATPase appears to serve a regulatory role in the activity of Na(+),K(+)-ATPase, we postulated that a difference in the phosphorylation of the alpha1-subunit may be found among the fibers. We utilized two well-characterized specific antibodies for the alpha1-subunit, namely the McK1 and alpha6F, to determine, by immunofluorescence, if the alpha1-subunit in rat skeletal muscle fiber is differentially phosphorylated. McK1 has the unique property that its binding to the alpha1-subunit is greatly reduced when Ser-18 is phosphorylated. Our data show that, in red gastrocnemius muscle, only a small number of the fibers were stained on the sarcolemmal membrane by McK1, while other fibers were almost completely devoid of any staining. By contrast, the staining pattern by McK1 in the white gastrocnemius muscle was mostly uniform. Immunostaining of serial sections using the alpha6F antibody showed that the alpha1-subunit is expressed in all fibers. Dephosphorylation of the tissue sections by phosphatase partially restored immunostaining of the alpha1-subunit by McK1. Fiber typing results showed that, in red gastrocnemius, those fibers stained positive for alpha1-subunit by McK1 are the Type I fibers, whereas those stained negative are the Type IIA, IID, and IIB fibers. With age, the number of fibers in red gastrocnemius stained positive for McK1 increased markedly in 30-month old rats compared to 6-month old rats. In conclusion, our result suggests that, in rats, the alpha1-subunit of the Na(+),K(+)-ATPase is differentially phosphorylated in the fibers of the red gastrocnemius muscle. Furthermore, advanced age is associated with an apparent decrease in the phosphorylation of the alpha1-subunit, in addition to the previously demonstrated increase in the levels of expression of the subunit.

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Year:  2007        PMID: 17457517     DOI: 10.1007/s11010-007-9479-5

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.842


  38 in total

1.  The Na+/K(+)-pump protects muscle excitability and contractility during exercise.

Authors:  O B Nielsen; T Clausen
Journal:  Exerc Sport Sci Rev       Date:  2000-10       Impact factor: 6.230

Review 2.  Mechanisms of sodium pump regulation.

Authors:  A G Therien; R Blostein
Journal:  Am J Physiol Cell Physiol       Date:  2000-09       Impact factor: 4.249

3.  Ionic mechanisms of excitation-induced regulation of Na+-K+-ATPase mRNA expression in isolated rat EDL muscle.

Authors:  K T Murphy; W A Macdonald; M J McKenna; T Clausen
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2005-12-15       Impact factor: 3.619

4.  Dopamine-induced endocytosis of Na+,K+-ATPase is initiated by phosphorylation of Ser-18 in the rat alpha subunit and Is responsible for the decreased activity in epithelial cells.

Authors:  A V Chibalin; G Ogimoto; C H Pedemonte; T A Pressley; A I Katz; E Féraille; P O Berggren; A M Bertorello
Journal:  J Biol Chem       Date:  1999-01-22       Impact factor: 5.157

Review 5.  Ion gradients and contractility in skeletal muscle: the role of active Na+, K+ transport.

Authors:  O B Nielsen; K Overgaard
Journal:  Acta Physiol Scand       Date:  1996-03

6.  Phosphorylation of Na,K-ATPase by protein kinase C at Ser18 occurs in intact cells but does not result in direct inhibition of ATP hydrolysis.

Authors:  M S Feschenko; K J Sweadner
Journal:  J Biol Chem       Date:  1997-07-11       Impact factor: 5.157

7.  Role of Na(+)-K+ pump and Na+ channel concentrations in the contractility of rat soleus muscle.

Authors:  A P Harrison; O B Nielsen; T Clausen
Journal:  Am J Physiol       Date:  1997-05

Review 8.  The regulation of the Na+,K+ pump in contracting skeletal muscle.

Authors:  O B Nielsen; A P Harrison
Journal:  Acta Physiol Scand       Date:  1998-03

9.  The significance of active Na+,K+ transport in the maintenance of contractility in rat skeletal muscle.

Authors:  O B Nielsen; T Clausen
Journal:  Acta Physiol Scand       Date:  1996-06

Review 10.  Cellular mechanisms of muscle fatigue.

Authors:  R H Fitts
Journal:  Physiol Rev       Date:  1994-01       Impact factor: 37.312

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  4 in total

1.  Na,K-ATPase activity in mouse muscle is regulated by AMPK and PGC-1α.

Authors:  Maria S Ingwersen; Michael Kristensen; Henriette Pilegaard; Jørgen F P Wojtaszewski; Erik A Richter; Carsten Juel
Journal:  J Membr Biol       Date:  2011-06-18       Impact factor: 1.843

2.  The alpha1 isoform of the Na+/K+ ATPase is up-regulated in dedifferentiated progenitor cells that mediate lens and retina regeneration in adult newts.

Authors:  M Natalia Vergara; Laura K Smiley; Katia Del Rio-Tsonis; Panagiotis A Tsonis
Journal:  Exp Eye Res       Date:  2008-08-08       Impact factor: 3.467

Review 3.  Effects of Age on Na(+),K(+)-ATPase Expression in Human and Rodent Skeletal Muscle.

Authors:  Victoria L Wyckelsma; Michael J McKenna
Journal:  Front Physiol       Date:  2016-08-02       Impact factor: 4.566

4.  Impaired AQP2 trafficking in Fxyd1 knockout mice: A role for FXYD1 in regulated vesicular transport.

Authors:  Elena Arystarkhova; Richard Bouley; Yi Bessie Liu; Kathleen J Sweadner
Journal:  PLoS One       Date:  2017-11-20       Impact factor: 3.240

  4 in total

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